Canonical Allele Identifier: PA104677
Gene: OCRL HGNC NCBI

Linked Data

ClinVar Variation Id: 10859
ClinVar RCV Id: RCV000011606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000267.2:p.His524Gln
CA255585
NM_000276.4:c.1572C>G
CA414616529
NM_000276.4:c.1572C>A